Section of Vascular Surgery, Dartmouth-Hitchcock Medical Center, Lebanon, NH.
The Dartmouth Institute for Health Policy and Clinical Practice, Lebanon, NH.
J Vasc Surg. 2014 Jun;59(6):1607-14. doi: 10.1016/j.jvs.2013.11.096. Epub 2014 Jan 24.
Although cilostazol is commonly used as an adjunct after peripheral vascular interventions, its efficacy remains uncertain. We assessed the effect of cilostazol on outcomes after peripheral vascular interventions using meta-analytic techniques.
We searched MEDLINE (1946-2012), Cochrane CENTRAL (1996-2012), and trial registries for studies comparing cilostazol in combination with antiplatelet therapy to antiplatelet therapy alone after peripheral vascular interventions. Treatment effects were reported as pooled risk/hazard ratio (HR) with random-effects models.
Two randomized trials and four retrospective cohorts involving 1522 patients met inclusion criteria. Across studies, mean age ranged from 65 to 76 years, and the majority of patients were male (64%-83%); mean follow-up ranged from 18 to 37 months. Most interventions were in the femoropopliteal segment, and overall, 68% of patients had stents placed. Pooled estimates demonstrated that the addition of cilostazol was associated with decreased restenosis (relative risk [RR], 0.71; 95% confidence interval [CI], 0.60-0.84; P < .001), improved amputation-free survival (HR, 0.63; 95% CI, 0.47-0.85; P = .002), improved limb salvage (HR, 0.42; 95% CI, 0.27-0.66; P < .001), and improved freedom from target lesion revascularization (RR, 1.36; 95% CI, 1.14-1.61; P < .001). There was no significant reduction in mortality among those receiving cilostazol (RR, 0.73; 95% CI, 0.45-1.19; P = .21).
The addition of cilostazol to antiplatelet therapy after peripheral vascular interventions is associated with a reduced risk of restenosis, amputation, and target lesion revascularization in our meta-analysis of six studies. Consideration of cilostazol as a medical adjunct after peripheral vascular interventions is warranted, presuming these findings are broadly generalizable.
尽管西洛他唑常用于外周血管介入治疗后,但它的疗效仍不确定。我们使用荟萃分析技术评估了西洛他唑对外周血管介入治疗后结局的影响。
我们检索了 MEDLINE(1946-2012 年)、Cochrane CENTRAL(1996-2012 年)和试验注册处,比较了外周血管介入治疗后西洛他唑联合抗血小板治疗与单独抗血小板治疗的研究。治疗效果以随机效应模型的合并风险/危害比(HR)报告。
两项随机试验和四项回顾性队列研究共纳入 1522 例患者。在这些研究中,平均年龄为 65-76 岁,大多数患者为男性(64%-83%);平均随访时间为 18-37 个月。大多数干预措施位于股浅动脉段,总体上有 68%的患者放置了支架。合并估计表明,添加西洛他唑与降低再狭窄(相对风险[RR],0.71;95%置信区间[CI],0.60-0.84;P<0.001)、提高截肢无生存(HR,0.63;95%CI,0.47-0.85;P=0.002)、改善肢体保存(HR,0.42;95%CI,0.27-0.66;P<0.001)和提高免于目标病变血运重建(RR,1.36;95%CI,1.14-1.61;P<0.001)有关。接受西洛他唑治疗的患者死亡率没有显著降低(RR,0.73;95%CI,0.45-1.19;P=0.21)。
我们对六项研究的荟萃分析表明,在外周血管介入治疗后添加西洛他唑可降低再狭窄、截肢和目标病变血运重建的风险。考虑将西洛他唑作为外周血管介入治疗后的一种医学辅助治疗是合理的,前提是这些发现具有广泛的普遍性。